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searching for MYH3 2 found (273 total)

alternate case: mYH3

Freeman–Sheldon syndrome (2,312 words) [view diff] exact match in snippet view article find links to article

Toydemir et al. (2006) showed that mutations in embryonic myosin heavy chain 3 (MYH3; MIM *160270), at 17p-13.1-pter, caused classic FSS phenotype, in their screening

Arthrogryposis (3,457 words) [view diff] exact match in snippet view article find links to article

distal arthrogryposis. Mutations in at least five genes (TNN12, TNNT3, TPM2, MYH3 and MYH8) could cause distal arthrogryposis. There could be also connective